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Bruton tyrosine kinase degradation as a therapeutic strategy for cancer
The covalent Bruton tyrosine kinase (BTK) inhibitor ibrutinib is highly efficacious against multiple B-cell malignancies. However, it is not selective for BTK, and multiple mechanisms of resistance, including the C481S-BTK mutation, can compromise its efficacy. We hypothesized that small-molecule–in...
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| Udgivet i: | Blood |
|---|---|
| Main Authors: | , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society of Hematology
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6396177/ https://ncbi.nlm.nih.gov/pubmed/30545835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2018-07-862953 |
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